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For Companies At a Glance
- Tasks: Support safety activities and manage safety reports for clinical development.
- Company: Join a world-renowned global pharmaceutical company with a focus on safety science.
- Benefits: Hybrid working, competitive salary, and opportunities for professional growth.
- Why this job: Make a real impact on patient safety and contribute to innovative healthcare solutions.
- Qualifications: Experience in signal detection and strong analytical skills required.
- Other info: Collaborative environment with a focus on high-quality safety deliverables.
The predicted salary is between 60000 - 84000 £ per year.
Overview
CPL Life Sciences are in collaboration with a world-renowned global pharmaceutical company who are seeking two new professionals at varying experience levels to join their Safety Science and Pharmacovigilance team. This role provides scientific safety oversight across the full lifecycle of investigational and marketed products.
Responsibilities
- Support safety activities in early and late-phase clinical development
- Conduct signal detection, evaluation, and contribute to risk‑benefit assessments
- Manage individual case safety reports (ICSRs) and prepare aggregate reports (e.g., DSURs, PBRERs)
- Participate in the preparation and review of regulatory submissions (INDs, NDAs, MAAs, etc.)
- Contribute to the development and maintenance of safety labeling and core safety documents
- Collaborate with internal teams and external partners to ensure high‑quality safety deliverables
- Provide safety input to study teams and participate in cross‑functional meetings
- Help prepare materials for safety committees (e.g., iDMCs, IMCs) and regulatory authorities
Working Conditions
Hybrid: North London 2 days per week on site, 3 days remote
Qualifications
Direct experience working with signal detection, aggregate reports and risk‑management plans for both clinical and post‑marketing activities. Strong analytical, communication and collaboration skills.
Associate Director Pharmacovigilance Scientist employer: Cpl Life Sciences
Contact Detail:
Cpl Life Sciences Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Associate Director Pharmacovigilance Scientist
✨Tip Number 1
Network like a pro! Reach out to professionals in the pharmacovigilance field on LinkedIn or at industry events. A friendly chat can open doors and give us insights into the company culture.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of signal detection and risk management plans. We want to show that we’re not just familiar with the terms, but we can also discuss them confidently.
✨Tip Number 3
Practice makes perfect! Conduct mock interviews with friends or mentors. This will help us articulate our experience with ICSR management and regulatory submissions smoothly.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who take that extra step.
We think you need these skills to ace Associate Director Pharmacovigilance Scientist
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience in pharmacovigilance and safety science. We want to see how your skills match the job description, so don’t be shy about showcasing your relevant achievements!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about pharmacovigilance and how you can contribute to our team. Keep it engaging and personal – we love to see your personality come through.
Showcase Your Analytical Skills: Since this role involves signal detection and risk assessments, make sure to highlight any relevant analytical projects or experiences. We’re looking for candidates who can demonstrate their ability to evaluate data effectively.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it’s super easy – just follow the prompts!
How to prepare for a job interview at Cpl Life Sciences
✨Know Your Pharmacovigilance Basics
Make sure you brush up on your knowledge of pharmacovigilance principles, especially around signal detection and risk management. Being able to discuss these topics confidently will show that you're well-prepared and understand the core responsibilities of the role.
✨Prepare for Scenario Questions
Expect questions that ask how you would handle specific safety scenarios or case reports. Think about past experiences where you've managed ICSR or contributed to aggregate reports, and be ready to share those examples in detail.
✨Familiarise Yourself with Regulatory Submissions
Since the role involves preparing regulatory submissions like INDs and NDAs, it’s crucial to know the basics of these processes. Research the latest guidelines and be prepared to discuss how you would approach these tasks.
✨Showcase Your Collaboration Skills
This position requires working closely with various teams. Be ready to talk about your experience collaborating with internal and external partners. Highlight specific projects where teamwork led to successful outcomes, as this will demonstrate your ability to contribute effectively in a cross-functional environment.
